Guidance: Use of International Standard ISO 10993-1, Biological Evaluation of Medical Devices, Part 1: Evaluation and Testing within a Risk Management Process

TitleGuidance: Use of International Standard ISO 10993-1, Biological Evaluation of Medical Devices, Part 1: Evaluation and Testing within a Risk Management Process
ToC Doc Use of International Standard ISO 10993-1, Biological Evaluation of Medical Devices, Part 1: Evaluation and Testing within a Risk Management Process
Docket Number2023-19402
Type Notice
Subject Guidance:
Use of International Standard ISO 10993-1, Biological Evaluation of Medical Devices, Part 1: Evaluation and Testing within a Risk Management Process
Publication Date2023-09-08
Last Updated Date 2023-09-07 08:15:11 -0400
Last Public Inspection2023-09-07
Filed At2023-09-07T08:45:00.000-04:00
PDF 2023-19402_PI.pdf (111936 bytes)
Download TXT / HTML / JSON
Number of Pages 7
Filing Typeregular
AgenciesFood and Drug Administration

You can find the raw source document below...

This site's data is aggregated programmatically and provided "as is" without any representations or warranties, express or implied. OFR.report is not affiliated with the Office of the Federal Register or the US government in any way.

© OFR.report 2021